Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Emily, Griffin"'
Autor:
Meredith L. Gore, Rowan Hilend, Jonathan O. Prell, Emily Griffin, John R. Macdonald, Burcu B. Keskin, Aaron Ferber, Bistra Dilkina
Publikováno v:
Big Earth Data, Vol 7, Iss 2, Pp 338-348 (2023)
ABSTRACTWildlife trafficking is a global phenomenon posing many negative impacts on socio-environmental systems. Scientific exploration of wildlife trafficking trends and the impact of interventions is significantly encumbered by a suite of data reus
Externí odkaz:
https://doaj.org/article/4ca16feaf881451982b1f401ebc153ac
Autor:
Daniel Liebzeit, Anna Krupp, Jacinda Bunch, Shalome Tonelli, Emily Griffin, Sarah McVeigh, Nai‐Ching Chi, Saida Jaboob, Lynn Nakad, Alicia I. Arbaje, Harleah Buck
Publikováno v:
Health Science Reports, Vol 6, Iss 5, Pp n/a-n/a (2023)
Abstract Background and Aims The population of older adults in rural areas is rising, and they experience higher rates of poverty and chronic illness, have poorer health behaviors, and experience different challenges than those in urban areas. This s
Externí odkaz:
https://doaj.org/article/dc2ba17ab4d4438cb6834d1157c06db7
Autor:
Lachlan A. Jolly, Euan Parnell, Alison E. Gardner, Mark A. Corbett, Luis A. Pérez-Jurado, Marie Shaw, Gaetan Lesca, Catherine Keegan, Michael C. Schneider, Emily Griffin, Felicitas Maier, Courtney Kiss, Andrea Guerin, Kathleen Crosby, Kenneth Rosenbaum, Pranoot Tanpaiboon, Sandra Whalen, Boris Keren, Julie McCarrier, Donald Basel, Simon Sadedin, Susan M. White, Martin B. Delatycki, Tjitske Kleefstra, Sébastien Küry, Alfredo Brusco, Elena Sukarova-Angelovska, Slavica Trajkova, Sehoun Yoon, Stephen A. Wood, Michael Piper, Peter Penzes, Jozef Gecz
Publikováno v:
npj Genomic Medicine, Vol 5, Iss 1, Pp 1-11 (2020)
Abstract USP9X is an X-chromosome gene that escapes X-inactivation. Loss or compromised function of USP9X leads to neurodevelopmental disorders in males and females. While males are impacted primarily by hemizygous partial loss-of-function missense v
Externí odkaz:
https://doaj.org/article/698c9b16e7d1463b82071a45d7227565
Autor:
Alexander Hsieh, Sarah U. Morton, Jon A. L. Willcox, Joshua M. Gorham, Angela C. Tai, Hongjian Qi, Steven DePalma, David McKean, Emily Griffin, Kathryn B. Manheimer, Daniel Bernstein, Richard W. Kim, Jane W. Newburger, George A. Porter, Deepak Srivastava, Martin Tristani-Firouzi, Martina Brueckner, Richard P. Lifton, Elizabeth Goldmuntz, Bruce D. Gelb, Wendy K. Chung, Christine E. Seidman, J. G. Seidman, Yufeng Shen
Publikováno v:
Genome Medicine, Vol 12, Iss 1, Pp 1-18 (2020)
Abstract Background The contribution of somatic mosaicism, or genetic mutations arising after oocyte fertilization, to congenital heart disease (CHD) is not well understood. Further, the relationship between mosaicism in blood and cardiovascular tiss
Externí odkaz:
https://doaj.org/article/b7f196ef4fc94a1c9c9e2a38f2b299d7
Autor:
Jose Fernández-Triana, Joel Buffam, Melanie Beaudin, Hannah Davis, Ana Fernández-Galliano, Emily Griffin, Shang-Yao Lin, Megan K. McAulay, Robin Richter, Freddy Rodriguez, Gergely Várkonyi
Publikováno v:
ZooKeys, Vol 691, Iss , Pp 49-101 (2017)
The Microgastrinae (Hymenoptera: Braconidae) from ten islands of the Canadian Arctic Archipelago (CAA) and Greenland were studied based on 2,183 specimens deposited in collections. We report a total of 33 species in six genera, more than doubling the
Externí odkaz:
https://doaj.org/article/942a4521808d464e8b81db3d91608f58
Autor:
Andrew Metcalfe, Helen Parsons, Nicholas Parsons, Jaclyn Brown, Josephine Fox, Elke Gemperlé Mannion, Aminul Haque, Charles Hutchinson, Rebecca Kearney, Iftekhar Khan, Tom Lawrence, James Mason, Nigel Stallard, Martin Underwood, Stephen Drew, Azra Arif, Susanne Arnold, Gev Bhabra, Sunayna Bora, Howard Bush, Jo Fox, Ceri Jones, Thomas Lawrence, Kerri McGowan, Chetan Modi, Bushra Rahman, Usama Rahman, Maria Ramirez, Marta Spocinska, Joanna Teuke, Varjithan Thayalan, Sumayyah Ul-Rahman, Aparna Viswanath, Iain Packham, Elizabeth Barnett, Rian Witham, Mark Crowther, Richard Murphy, Katherine Coates, Josephine Morley, Stephen Barnfield, Sukhdeep Gill, Alistair Jones, Ruth Halliday, Sarah Dunn, James Fagg, Peter Dacombe, Rajesh Nanda, Deborah Wilson, Lesley Boulton, Raymond Liow, Richard Jeavons, Andrea Meddes, Niel Kang, Leila Dehghani, Aileen Nacorda, Anuj Punnoose, Nicholas Ferran, Gbadebo Adewetan, Temi Adedoyin, Arun Pall, Matthew Sala, Tariq Zaman, Richard Hartley, Charif a-Sayyad, Luke Vamplew, Elizabeth Howe, Norbert Bokor, Steve Corbett, Robert Moverley, Elise Cox, Oliver Donaldson, Michael Jones, Diane Wood, Jess Perry, Alison Lewis, Linda Howard, Kate Beesley, Luke Harries, Ahmed Elmorsy, Katherine Wilcocks, Kate Shean, Sarah Diment, Helen Pidgeon, Victoria King, Soren Sjolin, Angharad Williams, Joanne Kellett, Lora Young, Michael Dunne, Tom Lockwood, Mark Curtis, Nashat Siddiqui, India Mckenley, Sarah Morrison, Charlotte Morrison, Tracey O'Brien, Isabel Bradley, Kenneth Lambatan, Cormac Kelly, Charlotte Perkins, Teresa Jones, Tessa Rowlands, Dawn Collins, Claire Nicholas, Claire Birch, Julie Lloyd -Evans, Pouya Akhbari, Jefin Jose Edakalathu, Campbell Hand, Andy Cole, Debbie Prince, Kerry Thorpe, Louise Rooke, Maria Baggot, Matt Morris, Dima Ivanova, David Baker, Tim Matthews, Jessica Falatoori, Heather Jarvis, Debbie Jones, Matthew Williams, Richard Evans, Huw Pullen, Gemma Hodkinson, Nicola Vannet, Alison Davey, Emma Poyser, Angela Hall, Hemang Mehta, Devi Prakash Tokola, Clare Connor, Caroline Jordan, Owain Ennis, Zohra Omar, Tracy Lewis, Angharad Lisa Owen, Andrew Morgan, Ravi Ponnada, Waheeb Al-Azzani, Carolyn Williams, Liam Knox, Harvinder Singh, Tracy Lee, Kathryn Robinson, Dileep Kumar, Alison Armstrong, Addie Majed, Mark Falworth, David Butt, Deborah Higgs, Will Rudge, Ben Hughes, Esther Hanison, Deirdre Brooking, Amit Patel, Andrew Symonds, Jenifer Gibson, Rodney Santiago, David Barlow, Joanne Lennon, Christopher Smith, Jane Hall, Emily Griffin, Rebecca Lear, William Thomas, David Rose, Janet Edkins, Helen Samuel, Hagen Jahnich, John Geoghegan, Ben Gooding, Siobhan Hudson, Jess Nightingale, Madhavan Papanna, Tom Briggs, Rebecca Pugh, Amy Neal, Lisa Warrem, Veronica Maxwell, Robert Chadwick, Thomas Jaki, Loretta Davies, Stephen Gwilym, Rod Taylor, Geoffrey Abel, John Graham, Christopher Littlewood, Angus Wallace, Anthony Howard
Publikováno v:
The Lancet. 399:1954-1963
New surgical procedures can expose patients to harm and should be carefully evaluated before widespread use. The InSpace balloon (Stryker, USA) is an innovative surgical device used to treat people with rotator cuff tears that cannot be repaired. We
Autor:
Meredith L. Gore, Emily Griffin, Bistra Dilkina, Aaron Ferber, Stanley E. Griffis, Burcu B. Keskin, John Macdonald
Publikováno v:
Proceedings of the National Academy of Sciences. 120
Wildlife trafficking, whether local or transnational in scope, undermines sustainable development efforts, degrades cultural resources, endangers species, erodes the local and global economy, and facilitates the spread of zoonotic diseases. Wildlife
Publikováno v:
Integration of Constraint Programming, Artificial Intelligence, and Operations Research ISBN: 9783031332708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::087ecd1457a196208c6053f1fdf4cef6
https://doi.org/10.1007/978-3-031-33271-5_30
https://doi.org/10.1007/978-3-031-33271-5_30
Autor:
Thomas Hays, Rebecca Hernan, Michele Disco, Emily Griffin, Nimrod Goldshtrom, Diana Vargas, Ganga Krishnamurthy, Atteeq U. Rehman, Amanda T. Wilson, Saurav Guha, Shruti Phadke, Volkan Okur, Dino Robinson, Vanessa Felice, Avinash Abhyankar, Vaidehi Jobanputra, Wendy K. Chung
BackgroundRapid genome sequencing (rGS) has been shown to improve the care of critically ill infants. Congenital heart disease (CHD) is a leading cause of infant mortality, and is often caused by genetic disorders, yet the utility of rGS has not been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77320068b01e40d3023ef138ebbf83c1
https://doi.org/10.1101/2022.12.16.22283479
https://doi.org/10.1101/2022.12.16.22283479
Autor:
Hagar Mor-Shaked, Simcha Yagel, Charles A. LeDuc, Emily Griffin, Hagit Daum, Wendy K. Chung, Vardiella Meiner, Jacob J. Hagen, Yoel Hirsch, Mythily Ganapathi
Publikováno v:
American Journal of Medical Genetics Part A. 188:336-342
Exome and genome sequencing were used to identify the genetic etiology of a severe neurodevelopmental disorder in two unrelated Ashkenazi Jewish families with three affected individuals. The clinical findings included a prenatal presentation of micro